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FDA 510(k)

Bone Screws dia. 5,0 mm

K-Number: K210717 · 2021-07-12

Decision Date2021-07-12
Product CodePHX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Bone Screws dia. 5,0 mm is a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2021-07-12 under approval number K210717. The device is classified under product code PHX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Bone Screws dia. 5,0 mm?

Bone Screws dia. 5,0 mm is a medical device that received FDA 510(k) clearance on 2021-07-12. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K210717.

When was Bone Screws dia. 5,0 mm approved by the FDA?

Bone Screws dia. 5,0 mm received FDA 510(k) clearance on 2021-07-12, under approval number K210717.

What company makes Bone Screws dia. 5,0 mm?

Bone Screws dia. 5,0 mm is manufactured by Lima Corporate S.P.A..

What is the FDA product code for Bone Screws dia. 5,0 mm?

The FDA product code for Bone Screws dia. 5,0 mm is PHX.

Other Devices by Lima Corporate S.P.A.

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Related Devices (Code: PHX)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.